Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. - Netravathi, Manjunath; Kumari, Renu; Kapoor, Saketh; Dakle, Pushkar; Dwivedi, Manish Kumar; Roy, Sumitabho Deb; Pandey, Paritosh; Saini, Jitender; Ramakrishna, Anil; Navalli, Devaraddi; Satishchandra, Parthasarathy; Pal, Pramod Kumar; et al. (BMC Medical Genetics, 2015)